CA2950423A1 - Compositions et procedes concernant des glycoformes universelles pour une efficacite d'anticorps amelioree - Google Patents
Compositions et procedes concernant des glycoformes universelles pour une efficacite d'anticorps amelioree Download PDFInfo
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Abstract
La présente invention concerne des glycoprotéines, en particulier des anticorps monoclonaux, comprenant une région Fc glycomodifiée, dans lesquelles ladite région Fc comprend un N-glycane optimisé ayant la structure de Sia2(a2-6)Gal2GlcNAc2Man3GlcNAc2 La région Fc glycomodifiée lie Fc?RIIA ou Fc?RIIIA avec une affinité plus élevée, par rapport à celle d'anticorps monoclonaux comparables comprenant la zone Fc de type sauvage. Les anticorps monoclonaux de l'invention sont particulièrement utiles dans la prévention, le traitement, ou l'amélioration d'un ou plusieurs symptômes associés à une maladie, un trouble, ou une infection dans lesquels une efficacité améliorée de la fonction cellulaire effectrice (par exemple, ADCC) médiée par Fc?R est souhaitée, par exemple, un cancer, une maladie auto-immune ou infectieuse, et dans l'amélioration de l'efficacité thérapeutique d'anticorps thérapeutiques dont l'effet est médié par ADCC.
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US201462003104P | 2014-05-27 | 2014-05-27 | |
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US62/110,338 | 2015-01-30 | ||
PCT/US2015/032745 WO2015184009A1 (fr) | 2014-05-27 | 2015-05-27 | Compositions et procédés concernant des glycoformes universelles pour une efficacité d'anticorps améliorée |
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CA2950423A1 true CA2950423A1 (fr) | 2015-12-03 |
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CA2950577A Pending CA2950577A1 (fr) | 2014-05-27 | 2015-05-27 | Fucosidase issue de bacteroides et ses procedes d'utilisation |
CA2950423A Pending CA2950423A1 (fr) | 2014-05-27 | 2015-05-27 | Compositions et procedes concernant des glycoformes universelles pour une efficacite d'anticorps amelioree |
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CA2950577A Pending CA2950577A1 (fr) | 2014-05-27 | 2015-05-27 | Fucosidase issue de bacteroides et ses procedes d'utilisation |
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US (4) | US10023892B2 (fr) |
EP (4) | EP3149161B1 (fr) |
JP (5) | JP6894239B2 (fr) |
KR (5) | KR20230033737A (fr) |
CN (3) | CN106661562A (fr) |
AU (3) | AU2015267052A1 (fr) |
CA (2) | CA2950577A1 (fr) |
DK (2) | DK3149045T3 (fr) |
FI (1) | FI3149045T3 (fr) |
IL (2) | IL249195B (fr) |
TW (2) | TWI654202B (fr) |
WO (2) | WO2015184009A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018133139A1 (fr) | 2017-01-21 | 2018-07-26 | 宁波知明生物科技有限公司 | Application de paeéniflorin-6'-o-benzène sulfonate en médecine pour le traitement du syndrome de sjögren |
US11377485B2 (en) * | 2009-12-02 | 2022-07-05 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7960139B2 (en) | 2007-03-23 | 2011-06-14 | Academia Sinica | Alkynyl sugar analogs for the labeling and visualization of glycoconjugates in cells |
WO2010009271A2 (fr) | 2008-07-15 | 2010-01-21 | Academia Sinica | Matrices de glycane sur des lames de verre revêtues d’aluminium de type ptfe et procédés associés |
US10087236B2 (en) | 2009-12-02 | 2018-10-02 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
WO2011130332A1 (fr) | 2010-04-12 | 2011-10-20 | Academia Sinica | Puces au glycane pour la recherche par criblage haut débit de virus |
GB201201314D0 (en) * | 2012-01-26 | 2012-03-07 | Isis Innovation | Composition |
US10130714B2 (en) | 2012-04-14 | 2018-11-20 | Academia Sinica | Enhanced anti-influenza agents conjugated with anti-inflammatory activity |
AU2013306098A1 (en) | 2012-08-18 | 2015-02-12 | Academia Sinica | Cell-permeable probes for identification and imaging of sialidases |
CN104902898B (zh) | 2012-12-07 | 2018-02-23 | 凯莫森特里克斯股份有限公司 | 二唑内酰胺 |
AR095196A1 (es) | 2013-03-15 | 2015-09-30 | Regeneron Pharma | Medio de cultivo celular libre de suero |
EP3013365B1 (fr) | 2013-06-26 | 2019-06-05 | Academia Sinica | Antigènes rm2 et leur utilisation |
WO2014210564A1 (fr) | 2013-06-27 | 2014-12-31 | Academia Sinica | Conjugués de glycane et leur utilisation |
CA2923579C (fr) | 2013-09-06 | 2023-09-05 | Academia Sinica | Activation des cellules humaines inkt a l'aide de glycolipides ayant des groupes glycolsyles modifies |
US10150818B2 (en) | 2014-01-16 | 2018-12-11 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US9982041B2 (en) | 2014-01-16 | 2018-05-29 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
EP3129767B1 (fr) | 2014-03-27 | 2021-09-01 | Academia Sinica | Composés de marquage réactifs et leurs utilisations |
AU2015267047A1 (en) | 2014-05-27 | 2017-01-05 | Academia Sinica | Anti-CD20 glycoantibodies and uses thereof |
JP7062361B2 (ja) | 2014-05-27 | 2022-05-06 | アカデミア シニカ | 抗her2糖操作抗体群およびその使用 |
AU2015267052A1 (en) | 2014-05-27 | 2016-12-15 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
US10118969B2 (en) * | 2014-05-27 | 2018-11-06 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
JP7063538B2 (ja) | 2014-05-28 | 2022-05-09 | アカデミア シニカ | 抗TNFα糖操作抗体群およびその使用 |
WO2016040369A2 (fr) | 2014-09-08 | 2016-03-17 | Academia Sinica | Activation des cellules inkt humaines par des glycolipides |
US10495645B2 (en) | 2015-01-16 | 2019-12-03 | Academia Sinica | Cancer markers and methods of use thereof |
US9975965B2 (en) | 2015-01-16 | 2018-05-22 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
WO2016118961A1 (fr) * | 2015-01-24 | 2016-07-28 | Academia Sinica | Marqueurs de cancer et leurs procédés d'utilisation |
CA2972072A1 (fr) | 2015-01-24 | 2016-07-28 | Academia Sinica | Nouveaux composes conjugues de glycane et leurs methodes d'utilisation |
EP3250590B1 (fr) * | 2015-01-30 | 2021-09-15 | Academia Sinica | Compositions et procédés concernant des glycoformes universelles pour une efficacité d'anticorps anti-ssea4 améliorée |
WO2016196740A1 (fr) * | 2015-06-02 | 2016-12-08 | The Rockefeller University | Anticorps tri-spécifiques pour traitement anti-vih |
TW201808978A (zh) | 2016-03-08 | 2018-03-16 | 中央研究院 | N-聚醣及其陣列之模組化合成方法 |
SG11201808626WA (en) * | 2016-04-07 | 2018-10-30 | Chemocentryx Inc | Reducing tumor burden by administering ccr1 antagonists in combination with pd-1 inhibitors or pd-l1 inhibitors |
AU2017316663B2 (en) | 2016-08-22 | 2024-02-22 | CHO Pharma Inc. | Antibodies, binding fragments, and methods of use |
EP3288086A1 (fr) | 2016-08-26 | 2018-02-28 | LG Electronics Inc. | Module de cellule solaire et son procédé de fabrication |
CA3048452C (fr) * | 2016-12-29 | 2021-06-15 | Development Center For Biotechnology | Procedes de preparation de conjugues glycoproteine-medicament |
US10260056B2 (en) | 2017-03-17 | 2019-04-16 | New England Biolabs, Inc. | Cleavage of fucose in N-glycans |
JP7265494B2 (ja) * | 2017-07-06 | 2023-04-26 | リジェネロン・ファーマシューティカルズ・インコーポレイテッド | 糖タンパク質を作製するための細胞培養方法 |
US12077792B2 (en) * | 2018-05-15 | 2024-09-03 | The Board Of Trustees Of The University Of Illinois | Engineered microorganisms for production of 2′fucosyllactose and l-fucose |
CN110760492A (zh) * | 2018-07-25 | 2020-02-07 | 复旦大学 | 一种岩藻糖苷酶及其在制备孟买型红细胞中的应用 |
WO2021026264A1 (fr) * | 2019-08-05 | 2021-02-11 | Cho Pharma, Inc. | Protéine de fusion pour le remodelage de la glycoforme d'anticorps |
JP7523789B2 (ja) | 2019-09-04 | 2024-07-29 | 独立行政法人国立病院機構 | 抗炎症性非フコシル化免疫グロブリン製剤及びその製造方法 |
TW202216771A (zh) * | 2020-06-26 | 2022-05-01 | 德商拜耳廠股份有限公司 | 用於治療應用之ccr8抗體 |
US20220143172A1 (en) * | 2020-11-06 | 2022-05-12 | CHO Pharma Inc. | Immune composition comprising antigen and glycoengineered antibody thereof |
CA3222409A1 (fr) * | 2021-06-07 | 2022-12-15 | Amgen Inc. | Utilisation de fucosidase pour controler le taux d'afucosylation de proteines glycosylees |
CN113960232B (zh) * | 2021-10-28 | 2024-02-20 | 苏州大学 | 一种基于唾液特异性岩藻糖基化结构糖谱及其检测方法和应用 |
CN116903738A (zh) * | 2022-08-02 | 2023-10-20 | 北京绿竹生物技术股份有限公司 | 一种低甘露糖型抗人肿瘤坏死因子-α单抗及其用途 |
CN116554330B (zh) * | 2023-07-04 | 2023-09-01 | 天津旷博同生生物技术有限公司 | 一种抗人cd24工程抗体及应用 |
Family Cites Families (399)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3773919A (en) | 1969-10-23 | 1973-11-20 | Du Pont | Polylactide-drug mixtures |
US3896111A (en) | 1973-02-20 | 1975-07-22 | Research Corp | Ansa macrolides |
US4151042A (en) | 1977-03-31 | 1979-04-24 | Takeda Chemical Industries, Ltd. | Method for producing maytansinol and its derivatives |
US4137230A (en) | 1977-11-14 | 1979-01-30 | Takeda Chemical Industries, Ltd. | Method for the production of maytansinoids |
USRE30985E (en) | 1978-01-01 | 1982-06-29 | Serum-free cell culture media | |
US4265814A (en) | 1978-03-24 | 1981-05-05 | Takeda Chemical Industries | Matansinol 3-n-hexadecanoate |
US4307016A (en) | 1978-03-24 | 1981-12-22 | Takeda Chemical Industries, Ltd. | Demethyl maytansinoids |
JPS5562090A (en) | 1978-10-27 | 1980-05-10 | Takeda Chem Ind Ltd | Novel maytansinoid compound and its preparation |
US4256746A (en) | 1978-11-14 | 1981-03-17 | Takeda Chemical Industries | Dechloromaytansinoids, their pharmaceutical compositions and method of use |
JPS55164687A (en) | 1979-06-11 | 1980-12-22 | Takeda Chem Ind Ltd | Novel maytansinoid compound and its preparation |
JPS5566585A (en) | 1978-11-14 | 1980-05-20 | Takeda Chem Ind Ltd | Novel maytansinoid compound and its preparation |
JPS55102583A (en) | 1979-01-31 | 1980-08-05 | Takeda Chem Ind Ltd | 20-acyloxy-20-demethylmaytansinoid compound |
JPS55162791A (en) | 1979-06-05 | 1980-12-18 | Takeda Chem Ind Ltd | Antibiotic c-15003pnd and its preparation |
JPS55164685A (en) | 1979-06-08 | 1980-12-22 | Takeda Chem Ind Ltd | Novel maytansinoid compound and its preparation |
JPS55164686A (en) | 1979-06-11 | 1980-12-22 | Takeda Chem Ind Ltd | Novel maytansinoid compound and its preparation |
US4309428A (en) | 1979-07-30 | 1982-01-05 | Takeda Chemical Industries, Ltd. | Maytansinoids |
JPS5645483A (en) | 1979-09-19 | 1981-04-25 | Takeda Chem Ind Ltd | C-15003phm and its preparation |
EP0028683A1 (fr) | 1979-09-21 | 1981-05-20 | Takeda Chemical Industries, Ltd. | Antibiotique C-15003 PHO et sa préparation |
JPS5645485A (en) | 1979-09-21 | 1981-04-25 | Takeda Chem Ind Ltd | Production of c-15003pnd |
US4270537A (en) | 1979-11-19 | 1981-06-02 | Romaine Richard A | Automatic hypodermic syringe |
US4376110A (en) | 1980-08-04 | 1983-03-08 | Hybritech, Incorporated | Immunometric assays using monoclonal antibodies |
WO1982001188A1 (fr) | 1980-10-08 | 1982-04-15 | Takeda Chemical Industries Ltd | Composes 4,5-deoxymaytansinoide et leur procede de preparation |
US4450254A (en) | 1980-11-03 | 1984-05-22 | Standard Oil Company | Impact improvement of high nitrile resins |
US4419446A (en) | 1980-12-31 | 1983-12-06 | The United States Of America As Represented By The Department Of Health And Human Services | Recombinant DNA process utilizing a papilloma virus DNA as a vector |
US4315929A (en) | 1981-01-27 | 1982-02-16 | The United States Of America As Represented By The Secretary Of Agriculture | Method of controlling the European corn borer with trewiasine |
US4313946A (en) | 1981-01-27 | 1982-02-02 | The United States Of America As Represented By The Secretary Of Agriculture | Chemotherapeutically active maytansinoids from Trewia nudiflora |
JPS57192389A (en) | 1981-05-20 | 1982-11-26 | Takeda Chem Ind Ltd | Novel maytansinoid |
US4596792A (en) | 1981-09-04 | 1986-06-24 | The Regents Of The University Of California | Safe vaccine for hepatitis containing polymerized serum albumin |
US4741900A (en) | 1982-11-16 | 1988-05-03 | Cytogen Corporation | Antibody-metal ion complexes |
US4601978A (en) | 1982-11-24 | 1986-07-22 | The Regents Of The University Of California | Mammalian metallothionein promoter system |
US4560655A (en) | 1982-12-16 | 1985-12-24 | Immunex Corporation | Serum-free cell culture medium and process for making same |
US4657866A (en) | 1982-12-21 | 1987-04-14 | Sudhir Kumar | Serum-free, synthetic, completely chemically defined tissue culture media |
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
US4767704A (en) | 1983-10-07 | 1988-08-30 | Columbia University In The City Of New York | Protein-free culture medium |
US4599230A (en) | 1984-03-09 | 1986-07-08 | Scripps Clinic And Research Foundation | Synthetic hepatitis B virus vaccine including both T cell and B cell determinants |
US4599231A (en) | 1984-03-09 | 1986-07-08 | Scripps Clinic And Research Foundation | Synthetic hepatitis B virus vaccine including both T cell and B cell determinants |
US4965199A (en) | 1984-04-20 | 1990-10-23 | Genentech, Inc. | Preparation of functional human factor VIII in mammalian cells using methotrexate based selection |
US4970198A (en) | 1985-10-17 | 1990-11-13 | American Cyanamid Company | Antitumor antibiotics (LL-E33288 complex) |
US4596556A (en) | 1985-03-25 | 1986-06-24 | Bioject, Inc. | Hypodermic injection apparatus |
US4601903A (en) | 1985-05-01 | 1986-07-22 | The United States Of America As Represented By The Department Of Health And Human Services | Vaccine against Neisseria meningitidis Group B serotype 2 invasive disease |
GB8516415D0 (en) | 1985-06-28 | 1985-07-31 | Celltech Ltd | Culture of animal cells |
US4676980A (en) | 1985-09-23 | 1987-06-30 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Target specific cross-linked heteroantibodies |
US4927762A (en) | 1986-04-01 | 1990-05-22 | Cell Enterprises, Inc. | Cell culture medium with antioxidant |
US5567610A (en) | 1986-09-04 | 1996-10-22 | Bioinvent International Ab | Method of producing human monoclonal antibodies and kit therefor |
US6024983A (en) | 1986-10-24 | 2000-02-15 | Southern Research Institute | Composition for delivering bioactive agents for immune response and its preparation |
US5075109A (en) | 1986-10-24 | 1991-12-24 | Southern Research Institute | Method of potentiating an immune response |
CA1283827C (fr) | 1986-12-18 | 1991-05-07 | Giorgio Cirelli | Dispositif pour l'injection de formules liquides |
IL85035A0 (en) | 1987-01-08 | 1988-06-30 | Int Genetic Eng | Polynucleotide molecule,a chimeric antibody with specificity for human b cell surface antigen,a process for the preparation and methods utilizing the same |
US5079233A (en) | 1987-01-30 | 1992-01-07 | American Cyanamid Company | N-acyl derivatives of the LL-E33288 antitumor antibiotics, composition and methods for using the same |
GB8704027D0 (en) | 1987-02-20 | 1987-03-25 | Owen Mumford Ltd | Syringe needle combination |
AU600575B2 (en) | 1987-03-18 | 1990-08-16 | Sb2, Inc. | Altered antibodies |
US4849222A (en) | 1987-03-24 | 1989-07-18 | The Procter & Gamble Company | Mixtures for treating hypercholesterolemia |
US4790824A (en) | 1987-06-19 | 1988-12-13 | Bioject, Inc. | Non-invasive hypodermic injection device |
US4941880A (en) | 1987-06-19 | 1990-07-17 | Bioject, Inc. | Pre-filled ampule and non-invasive hypodermic injection device assembly |
US4940460A (en) | 1987-06-19 | 1990-07-10 | Bioject, Inc. | Patient-fillable and non-invasive hypodermic injection device assembly |
US4975278A (en) | 1988-02-26 | 1990-12-04 | Bristol-Myers Company | Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells |
US5004697A (en) | 1987-08-17 | 1991-04-02 | Univ. Of Ca | Cationized antibodies for delivery through the blood-brain barrier |
US5770701A (en) | 1987-10-30 | 1998-06-23 | American Cyanamid Company | Process for preparing targeted forms of methyltrithio antitumor agents |
US5053394A (en) | 1988-09-21 | 1991-10-01 | American Cyanamid Company | Targeted forms of methyltrithio antitumor agents |
US5606040A (en) | 1987-10-30 | 1997-02-25 | American Cyanamid Company | Antitumor and antibacterial substituted disulfide derivatives prepared from compounds possessing a methyl-trithio group |
JP2670680B2 (ja) | 1988-02-24 | 1997-10-29 | 株式会社ビーエムジー | 生理活性物質含有ポリ乳酸系微小球およびその製造法 |
US5339163A (en) | 1988-03-16 | 1994-08-16 | Canon Kabushiki Kaisha | Automatic exposure control device using plural image plane detection areas |
JPH01287029A (ja) | 1988-05-13 | 1989-11-17 | Mect Corp | 新規抗ウィルス剤 |
ATE135397T1 (de) | 1988-09-23 | 1996-03-15 | Cetus Oncology Corp | Zellenzuchtmedium für erhöhtes zellenwachstum, zur erhöhung der langlebigkeit und expression der produkte |
GB8823869D0 (en) | 1988-10-12 | 1988-11-16 | Medical Res Council | Production of antibodies |
FR2638359A1 (fr) | 1988-11-03 | 1990-05-04 | Tino Dalto | Guide de seringue avec reglage de la profondeur de penetration de l'aiguille dans la peau |
US5175384A (en) | 1988-12-05 | 1992-12-29 | Genpharm International | Transgenic mice depleted in mature t-cells and methods for making transgenic mice |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
DE3920358A1 (de) | 1989-06-22 | 1991-01-17 | Behringwerke Ag | Bispezifische und oligospezifische, mono- und oligovalente antikoerperkonstrukte, ihre herstellung und verwendung |
DK0479909T3 (da) | 1989-06-29 | 1997-04-07 | Medarex Inc | Bispecifikke reagenser til AIDS-behandling |
US5690938A (en) | 1989-07-07 | 1997-11-25 | Oravax, Inc. | Oral immunization with multiple particulate antigen delivery system |
US5518725A (en) | 1989-09-25 | 1996-05-21 | University Of Utah Research Foundation | Vaccine compositions and method for induction of mucosal immune response via systemic vaccination |
CA2026147C (fr) | 1989-10-25 | 2006-02-07 | Ravi J. Chari | Agents cytotoxiques comprenant des maytansinoides et leur usage therapeutique |
US5208020A (en) | 1989-10-25 | 1993-05-04 | Immunogen Inc. | Cytotoxic agents comprising maytansinoids and their therapeutic use |
US5238843A (en) | 1989-10-27 | 1993-08-24 | Genencor International, Inc. | Method for cleaning a surface on which is bound a glycoside-containing substance |
US5312335A (en) | 1989-11-09 | 1994-05-17 | Bioject Inc. | Needleless hypodermic injection device |
US5064413A (en) | 1989-11-09 | 1991-11-12 | Bioject, Inc. | Needleless hypodermic injection device |
ATE139258T1 (de) | 1990-01-12 | 1996-06-15 | Cell Genesys Inc | Erzeugung xenogener antikörper |
US5061620A (en) | 1990-03-30 | 1991-10-29 | Systemix, Inc. | Human hematopoietic stem cell |
US5268164A (en) | 1990-04-23 | 1993-12-07 | Alkermes, Inc. | Increasing blood-brain barrier permeability with permeabilizer peptides |
US5112596A (en) | 1990-04-23 | 1992-05-12 | Alkermes, Inc. | Method for increasing blood-brain barrier permeability by administering a bradykinin agonist of blood-brain barrier permeability |
BR9106374A (pt) | 1990-04-24 | 1993-03-30 | Univ Newcastle Res Ass | Vacina oral e processo de extrair uma imunoresponsta em um mamifero |
CZ288492B6 (en) | 1990-04-24 | 2001-06-13 | Biota Scient Management | Derivatives of alpha-D-neuraminic acid, process of their preparation, their use and pharmaceutical preparations based thereon |
US5229275A (en) | 1990-04-26 | 1993-07-20 | Akzo N.V. | In-vitro method for producing antigen-specific human monoclonal antibodies |
US5427908A (en) | 1990-05-01 | 1995-06-27 | Affymax Technologies N.V. | Recombinant library screening methods |
DE69132709T2 (de) | 1990-06-29 | 2002-06-20 | Large Scale Biology Corp., Vacaville | Melaninproduktion durch transformierte mikroorganismen |
US5190521A (en) | 1990-08-22 | 1993-03-02 | Tecnol Medical Products, Inc. | Apparatus and method for raising a skin wheal and anesthetizing skin |
US5633425A (en) | 1990-08-29 | 1997-05-27 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
US5661016A (en) | 1990-08-29 | 1997-08-26 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
ATE300615T1 (de) | 1990-08-29 | 2005-08-15 | Genpharm Int | Transgene mäuse fähig zur produktion heterologer antikörper |
US5545806A (en) | 1990-08-29 | 1996-08-13 | Genpharm International, Inc. | Ransgenic non-human animals for producing heterologous antibodies |
US5625126A (en) | 1990-08-29 | 1997-04-29 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
US5714374A (en) | 1990-09-12 | 1998-02-03 | Rutgers University | Chimeric rhinoviruses |
US5122469A (en) | 1990-10-03 | 1992-06-16 | Genentech, Inc. | Method for culturing Chinese hamster ovary cells to improve production of recombinant proteins |
WO1992006691A1 (fr) | 1990-10-19 | 1992-04-30 | Biota Scientific Management Pty. Ltd. | Composes anti-viraux qui lient le site actif de la neuraminidase de la grippe et presentent une activite in vivo contre l'orthomixovirus et le paramyxovirus |
US5508192A (en) | 1990-11-09 | 1996-04-16 | Board Of Regents, The University Of Texas System | Bacterial host strains for producing proteolytically sensitive polypeptides |
US5264365A (en) | 1990-11-09 | 1993-11-23 | Board Of Regents, The University Of Texas System | Protease-deficient bacterial strains for production of proteolytically sensitive polypeptides |
ATE164395T1 (de) | 1990-12-03 | 1998-04-15 | Genentech Inc | Verfahren zur anreicherung von proteinvarianten mit geänderten bindungseigenschaften |
US5527288A (en) | 1990-12-13 | 1996-06-18 | Elan Medical Technologies Limited | Intradermal drug delivery device and method for intradermal delivery of drugs |
US5571894A (en) | 1991-02-05 | 1996-11-05 | Ciba-Geigy Corporation | Recombinant antibodies specific for a growth factor receptor |
AU1991592A (en) | 1991-04-30 | 1992-12-21 | Alkermes, Inc. | Cationized antibodies against intracellular proteins |
ATE255131T1 (de) | 1991-06-14 | 2003-12-15 | Genentech Inc | Humanisierter heregulin antikörper |
GB9114948D0 (en) | 1991-07-11 | 1991-08-28 | Pfizer Ltd | Process for preparing sertraline intermediates |
GB9118204D0 (en) | 1991-08-23 | 1991-10-09 | Weston Terence E | Needle-less injector |
SE9102652D0 (sv) | 1991-09-13 | 1991-09-13 | Kabi Pharmacia Ab | Injection needle arrangement |
CA2116774C (fr) | 1991-09-19 | 2003-11-11 | Paul J. Carter | Expression dans e. coli de fragments d'anticorps ayant au moins une cysteine presente sous forme de thiol libre. utilisation pour la production d'anticorps f(ab') bifonctionnels |
US5565332A (en) | 1991-09-23 | 1996-10-15 | Medical Research Council | Production of chimeric antibodies - a combinatorial approach |
DE69229477T2 (de) | 1991-09-23 | 1999-12-09 | Cambridge Antibody Technology Ltd., Melbourn | Methoden zur Herstellung humanisierter Antikörper |
US5362852A (en) | 1991-09-27 | 1994-11-08 | Pfizer Inc. | Modified peptide derivatives conjugated at 2-hydroxyethylamine moieties |
US5587458A (en) | 1991-10-07 | 1996-12-24 | Aronex Pharmaceuticals, Inc. | Anti-erbB-2 antibodies, combinations thereof, and therapeutic and diagnostic uses thereof |
US5288502A (en) | 1991-10-16 | 1994-02-22 | The University Of Texas System | Preparation and uses of multi-phase microspheres |
WO1993008829A1 (fr) | 1991-11-04 | 1993-05-13 | The Regents Of The University Of California | Compositions induisant la destruction de cellules infectees par l'hiv |
CA2122719A1 (fr) | 1991-11-19 | 1993-05-27 | Jack M. Gwaltney, Jr. | Traitement du rhume commun par l'antimediateur combine virostatique (covam) |
JPH0826057B2 (ja) | 1992-01-16 | 1996-03-13 | 株式会社ディ・ディ・エス研究所 | シアル酸オリゴ糖誘導体及び微粒子キャリヤー |
US5667988A (en) | 1992-01-27 | 1997-09-16 | The Scripps Research Institute | Methods for producing antibody libraries using universal or randomized immunoglobulin light chains |
ATE503496T1 (de) | 1992-02-06 | 2011-04-15 | Novartis Vaccines & Diagnostic | Biosynthetisches bindeprotein für tumormarker |
US5328483A (en) | 1992-02-27 | 1994-07-12 | Jacoby Richard M | Intradermal injection device with medication and needle guard |
US5733743A (en) | 1992-03-24 | 1998-03-31 | Cambridge Antibody Technology Limited | Methods for producing members of specific binding pairs |
US5326856A (en) | 1992-04-09 | 1994-07-05 | Cytogen Corporation | Bifunctional isothiocyanate derived thiocarbonyls as ligands for metal binding |
ZA932522B (en) | 1992-04-10 | 1993-12-20 | Res Dev Foundation | Immunotoxins directed against c-erbB-2(HER/neu) related surface antigens |
JP2904647B2 (ja) | 1992-06-12 | 1999-06-14 | 株式会社蛋白工学研究所 | 5−ブロム−4−クロロインド−3−イル−2−シアル酸の製造方法 |
PT651805E (pt) | 1992-07-17 | 2007-02-28 | Dana Farber Cancer Inst Inc | Método de ligação intracelular de moléculas-alvo |
US5383851A (en) | 1992-07-24 | 1995-01-24 | Bioject Inc. | Needleless hypodermic injection device |
WO1994002178A1 (fr) | 1992-07-27 | 1994-02-03 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Ciblage de liposomes sur la barriere hemato-encephalique |
AU668423B2 (en) | 1992-08-17 | 1996-05-02 | Genentech Inc. | Bispecific immunoadhesins |
US5569189A (en) | 1992-09-28 | 1996-10-29 | Equidyne Systems, Inc. | hypodermic jet injector |
DE69328435T2 (de) | 1992-10-22 | 2000-09-14 | Kirin Beer K.K., Tokio/Tokyo | Neues sphingolglycolipid und verwendung davon |
US5807722A (en) | 1992-10-30 | 1998-09-15 | Bioengineering Resources, Inc. | Biological production of acetic acid from waste gases with Clostridium ljungdahlii |
US5334144A (en) | 1992-10-30 | 1994-08-02 | Becton, Dickinson And Company | Single use disposable needleless injector |
US5736137A (en) | 1992-11-13 | 1998-04-07 | Idec Pharmaceuticals Corporation | Therapeutic application of chimeric and radiolabeled antibodies to human B lymphocyte restricted differentiation antigen for treatment of B cell lymphoma |
ATE196606T1 (de) | 1992-11-13 | 2000-10-15 | Idec Pharma Corp | Therapeutische verwendung von chimerischen und markierten antikörpern, die gegen ein differenzierung-antigen gerichtet sind, dessen expression auf menschliche b lymphozyt beschränkt ist, für die behandlung von b-zell-lymphoma |
US5635483A (en) | 1992-12-03 | 1997-06-03 | Arizona Board Of Regents Acting On Behalf Of Arizona State University | Tumor inhibiting tetrapeptide bearing modified phenethyl amides |
JP3523285B2 (ja) * | 1993-01-22 | 2004-04-26 | 雪印乳業株式会社 | 糖分解酵素の製造法 |
US5780588A (en) | 1993-01-26 | 1998-07-14 | Arizona Board Of Regents | Elucidation and synthesis of selected pentapeptides |
US5374541A (en) | 1993-05-04 | 1994-12-20 | The Scripps Research Institute | Combined use of β-galactosidase and sialyltransferase coupled with in situ regeneration of CMP-sialic acid for one pot synthesis of oligosaccharides |
US20020037517A1 (en) | 1993-05-28 | 2002-03-28 | Hutchens T. William | Methods for sequencing biopolymers |
CA2163345A1 (fr) | 1993-06-16 | 1994-12-22 | Susan Adrienne Morgan | Anticorps |
AU7980794A (en) | 1993-10-22 | 1995-05-08 | Genentech Inc. | Methods and compositions for microencapsulation of antigens for use as vaccines |
US5369017A (en) | 1994-02-04 | 1994-11-29 | The Scripps Research Institute | Process for solid phase glycopeptide synthesis |
EP0746564B1 (fr) | 1994-02-25 | 1998-12-02 | E.I. Du Pont De Nemours And Company | Acides sialiques 4-n-substitues et leurs sialosides |
WO1995024176A1 (fr) | 1994-03-07 | 1995-09-14 | Bioject, Inc. | Dispositif de remplissage d'ampoule |
US5466220A (en) | 1994-03-08 | 1995-11-14 | Bioject, Inc. | Drug vial mixing and transfer device |
US5773001A (en) | 1994-06-03 | 1998-06-30 | American Cyanamid Company | Conjugates of methyltrithio antitumor agents and intermediates for their synthesis |
US5622701A (en) | 1994-06-14 | 1997-04-22 | Protein Design Labs, Inc. | Cross-reacting monoclonal antibodies specific for E- and P-selectin |
JP3053873B2 (ja) | 1994-08-12 | 2000-06-19 | イムノメディクス,インコーポレイテッド | B細胞リンパ腫細胞および白血病細胞に特異的な免疫結合体およびヒト化抗体 |
US5639635A (en) | 1994-11-03 | 1997-06-17 | Genentech, Inc. | Process for bacterial production of polypeptides |
CA2207869A1 (fr) | 1994-12-02 | 1996-06-06 | Chiron Corporation | Methode permettant d'induire une reponse immunitaire avec un anticorps bispecifique |
US5663149A (en) | 1994-12-13 | 1997-09-02 | Arizona Board Of Regents Acting On Behalf Of Arizona State University | Human cancer inhibitory pentapeptide heterocyclic and halophenyl amides |
US5599302A (en) | 1995-01-09 | 1997-02-04 | Medi-Ject Corporation | Medical injection system and method, gas spring thereof and launching device using gas spring |
US5840523A (en) | 1995-03-01 | 1998-11-24 | Genetech, Inc. | Methods and compositions for secretion of heterologous polypeptides |
US5731168A (en) | 1995-03-01 | 1998-03-24 | Genentech, Inc. | Method for making heteromultimeric polypeptides |
US6673533B1 (en) | 1995-03-10 | 2004-01-06 | Meso Scale Technologies, Llc. | Multi-array multi-specific electrochemiluminescence testing |
US5641870A (en) | 1995-04-20 | 1997-06-24 | Genentech, Inc. | Low pH hydrophobic interaction chromatography for antibody purification |
US5869046A (en) | 1995-04-14 | 1999-02-09 | Genentech, Inc. | Altered polypeptides with increased half-life |
JPH11511238A (ja) | 1995-04-25 | 1999-09-28 | イロリ | 遠隔プログラム可能なメモリ付きマトリックス及びその使用 |
EP0822830B1 (fr) | 1995-04-27 | 2008-04-02 | Amgen Fremont Inc. | Anticorps anti-IL-8 dérivés de xenosouris immunisées |
CA2219486A1 (fr) | 1995-04-28 | 1996-10-31 | Abgenix, Inc. | Anticorps humains derives de xeno-souris immunisees |
US5730723A (en) | 1995-10-10 | 1998-03-24 | Visionary Medical Products Corporation, Inc. | Gas pressured needle-less injection device and method |
US5837234A (en) | 1995-06-07 | 1998-11-17 | Cytotherapeutics, Inc. | Bioartificial organ containing cells encapsulated in a permselective polyether suflfone membrane |
US6265150B1 (en) | 1995-06-07 | 2001-07-24 | Becton Dickinson & Company | Phage antibodies |
US5712374A (en) | 1995-06-07 | 1998-01-27 | American Cyanamid Company | Method for the preparation of substantiallly monomeric calicheamicin derivative/carrier conjugates |
US5714586A (en) | 1995-06-07 | 1998-02-03 | American Cyanamid Company | Methods for the preparation of monomeric calicheamicin derivative/carrier conjugates |
WO1997005267A2 (fr) | 1995-07-26 | 1997-02-13 | Maxim Pharmaceuticals | Apport de polynucleotides dans les muqueuses |
DE19544393A1 (de) | 1995-11-15 | 1997-05-22 | Hoechst Schering Agrevo Gmbh | Synergistische herbizide Mischungen |
US5893397A (en) | 1996-01-12 | 1999-04-13 | Bioject Inc. | Medication vial/syringe liquid-transfer apparatus |
US6027888A (en) | 1996-04-05 | 2000-02-22 | Board Of Regents, The University Of Texas System | Methods for producing soluble, biologically-active disulfide-bond containing eukaryotic proteins in bacterial cells |
GB9607549D0 (en) | 1996-04-11 | 1996-06-12 | Weston Medical Ltd | Spring-powered dispensing device |
US5922845A (en) | 1996-07-11 | 1999-07-13 | Medarex, Inc. | Therapeutic multispecific compounds comprised of anti-Fcα receptor antibodies |
US6340702B1 (en) | 1996-07-22 | 2002-01-22 | Sankyo Company, Limited | Neuraminic acid derivatives, their preparation and their medical use |
US6506564B1 (en) | 1996-07-29 | 2003-01-14 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
EA001603B1 (ru) | 1996-11-14 | 2001-06-25 | Байота Сайентифик Менеджмент Пти Лтд. | Новые соединения и методы их применения |
EP2305027B1 (fr) | 1996-12-03 | 2014-07-02 | Amgen Fremont Inc. | Mammifères trangèniques obtenus par génie génétique contenant des loci des immunoglobulines humaines qui comprennent plusieurs régions de VH et de Vkappa, et anticorps aussi obtenus. |
TW555562B (en) | 1996-12-27 | 2003-10-01 | Kirin Brewery | Method for activation of human antigen-presenting cells, activated human antigen-presenting cells and use thereof |
EP0970114B1 (fr) | 1997-04-18 | 2006-07-12 | Novartis AG | Neoglycoproteines |
US5993412A (en) | 1997-05-19 | 1999-11-30 | Bioject, Inc. | Injection apparatus |
US6083715A (en) | 1997-06-09 | 2000-07-04 | Board Of Regents, The University Of Texas System | Methods for producing heterologous disulfide bond-containing polypeptides in bacterial cells |
JPH1135593A (ja) | 1997-07-18 | 1999-02-09 | Daikin Ind Ltd | 2−フルオロフコシル−n−アロイルグルコサミン誘導体及びその中間物、並びにそれらの製造方法 |
TW480247B (en) | 1997-12-12 | 2002-03-21 | Gilead Sciences Inc | Novel compounds useful as neuraminidase inhibitors and pharmaceutical compositions containing same |
IT1298087B1 (it) | 1998-01-08 | 1999-12-20 | Fiderm S R L | Dispositivo per il controllo della profondita' di penetrazione di un ago, in particolare applicabile ad una siringa per iniezioni |
AU765703B2 (en) | 1998-03-27 | 2003-09-25 | Bruce J. Bryan | Luciferases, fluorescent proteins, nucleic acids encoding the luciferases and fluorescent proteins and the use thereof in diagnostics, high throughput screening and novelty items |
AU3369999A (en) | 1998-04-02 | 1999-10-25 | Genentech Inc. | Antibody variants and fragments thereof |
AU3657899A (en) | 1998-04-20 | 1999-11-08 | James E. Bailey | Glycosylation engineering of antibodies for improving antibody-dependent cellular cytotoxicity |
US6455571B1 (en) | 1998-04-23 | 2002-09-24 | Abbott Laboratories | Inhibitors of neuraminidases |
DE69930424T2 (de) | 1998-05-06 | 2006-12-14 | Genentech, Inc., South San Francisco | Anti-HER2 Antikörperzusammensetzung |
JP3773153B2 (ja) | 1998-05-29 | 2006-05-10 | 独立行政法人理化学研究所 | シアル酸誘導体 |
US6528286B1 (en) | 1998-05-29 | 2003-03-04 | Genentech, Inc. | Mammalian cell culture process for producing glycoproteins |
DE69905832T2 (de) | 1998-09-18 | 2004-02-05 | Massachusetts Institute Of Technology, Cambridge | Biologische Verwendungen von halbleitenden Nanokristallen |
FR2783523B1 (fr) * | 1998-09-21 | 2006-01-20 | Goemar Lab Sa | Fuco-oligosaccharides, enzyme pour leur preparation a partir des fucanes, bacterie productrice de l'enzyme et applications des fuco-oligosaccharides a la protection des plantes |
US6994966B2 (en) | 2000-02-17 | 2006-02-07 | Glycominds Ltd. | Combinatorial complex carbohydrate libraries and methods for the manufacture and uses thereof |
US6696304B1 (en) | 1999-02-24 | 2004-02-24 | Luminex Corporation | Particulate solid phase immobilized protein quantitation |
AUPP913999A0 (en) | 1999-03-12 | 1999-04-01 | Biota Scientific Management Pty Ltd | Novel chemical compounds and their use |
US7090973B1 (en) * | 1999-04-09 | 2006-08-15 | Oscient Pharmaceuticals Corporation | Nucleic acid sequences relating to Bacteroides fragilis for diagnostics and therapeutics |
US7854934B2 (en) | 1999-08-20 | 2010-12-21 | Sloan-Kettering Institute For Cancer Research | Glycoconjugates, glycoamino acids, intermediates thereto, and uses thereof |
US6824780B1 (en) | 1999-10-29 | 2004-11-30 | Genentech, Inc. | Anti-tumor antibody compositions and methods of use |
AUPQ422399A0 (en) | 1999-11-24 | 1999-12-16 | University Of New South Wales, The | Method of screening transformed or transfected cells |
US6727356B1 (en) | 1999-12-08 | 2004-04-27 | Epoch Pharmaceuticals, Inc. | Fluorescent quenching detection reagents and methods |
US7019129B1 (en) | 2000-05-09 | 2006-03-28 | Biosearch Technologies, Inc. | Dark quenchers for donor-acceptor energy transfer |
US7863020B2 (en) | 2000-06-28 | 2011-01-04 | Glycofi, Inc. | Production of sialylated N-glycans in lower eukaryotes |
US6514221B2 (en) | 2000-07-27 | 2003-02-04 | Brigham And Women's Hospital, Inc. | Blood-brain barrier opening |
AU2001286930A1 (en) | 2000-08-30 | 2002-03-13 | The Board Of Trustees Of The Leland Stanford Junior University | Glucocorticoid blocking agents for increasing blood-brain barrier permeability |
AUPR001000A0 (en) | 2000-09-08 | 2000-10-05 | Biota Scientific Management Pty Ltd | Novel chemical compounds and their use |
US7034036B2 (en) | 2000-10-30 | 2006-04-25 | Pain Therapeutics, Inc. | Inhibitors of ABC drug transporters at the blood-brain barrier |
US20030083299A1 (en) | 2000-11-04 | 2003-05-01 | Ferguson Ian A. | Non-invasive delivery of polypeptides through the blood-brain barrier |
JP2002153272A (ja) | 2000-11-24 | 2002-05-28 | Inst Of Physical & Chemical Res | 生体分子マイクロアレイ |
US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
AU2002338446A1 (en) | 2001-01-23 | 2002-11-05 | University Of Rochester Medical Center | Methods of producing or identifying intrabodies in eukaryotic cells |
US6884869B2 (en) | 2001-04-30 | 2005-04-26 | Seattle Genetics, Inc. | Pentapeptide compounds and uses related thereto |
DE10121982B4 (de) | 2001-05-05 | 2008-01-24 | Lts Lohmann Therapie-Systeme Ag | Nanopartikel aus Protein mit gekoppeltem Apolipoprotein E zur Überwindung der Blut-Hirn-Schranke und Verfahren zu ihrer Herstellung |
JP2002371087A (ja) | 2001-06-15 | 2002-12-26 | Mitsubishi Chemicals Corp | 有機ホスホン酸 |
JP4317010B2 (ja) | 2001-07-25 | 2009-08-19 | ピーディーエル バイオファーマ,インコーポレイティド | IgG抗体の安定な凍結乾燥医薬製剤 |
WO2003009815A2 (fr) | 2001-07-25 | 2003-02-06 | Biomarin Pharmaceutical Inc. | Compositions et procedes de modulation du transport a travers la barriere hematho-encephalique |
CN1561389A (zh) | 2001-07-25 | 2005-01-05 | 纽约大学 | 糖基神经酰胺作为用于抗传染病和癌症的疫苗的佐剂的用途 |
CA2455365C (fr) | 2001-08-03 | 2014-07-29 | Glycart Biotechnology Ag | Variants de glycosylation d'anticorps presentant une cytotoxicite cellulaire accrue dependante des anticorps |
WO2003031464A2 (fr) | 2001-10-10 | 2003-04-17 | Neose Technologies, Inc. | Remodelage et glycoconjugaison de peptides |
US7732002B2 (en) | 2001-10-19 | 2010-06-08 | Cabot Corporation | Method for the fabrication of conductive electronic features |
AUPR879601A0 (en) | 2001-11-09 | 2001-12-06 | Biota Scientific Management Pty Ltd | Novel chemical compounds and their use |
US6873914B2 (en) | 2001-11-21 | 2005-03-29 | Icoria, Inc. | Methods and systems for analyzing complex biological systems |
WO2003068821A2 (fr) | 2002-02-14 | 2003-08-21 | Immunomedics, Inc. | Anticorps anti-cd20 et proteines hybrides desdits anticorps, et methodes d'utilisation |
US20030162695A1 (en) | 2002-02-27 | 2003-08-28 | Schatzberg Alan F. | Glucocorticoid blocking agents for increasing blood-brain barrier permeability |
US7317091B2 (en) | 2002-03-01 | 2008-01-08 | Xencor, Inc. | Optimized Fc variants |
AU2003219277A1 (en) | 2002-03-14 | 2003-09-29 | Medical Research Council | Intracellular antibodies |
DE60328481D1 (de) | 2002-05-14 | 2009-09-03 | Novartis Vaccines & Diagnostic | Schleimhautapplizierter impfstoff, der das adjuvanz chitosan und menigokokkenantigene enthält |
WO2004005313A2 (fr) | 2002-07-08 | 2004-01-15 | Pliva - Istrazivacki Institut D.O.O. | Nouveaux composes, compositions en tant que porteurs pour molecules actives anti-inflammatoires steroidiennes/non-steroidiennes, antineoplasiques et antivirales |
US20080070324A1 (en) | 2002-07-15 | 2008-03-20 | Floyd Alton D | Quantity control device for microscope slide staining assays |
EP1391213A1 (fr) | 2002-08-21 | 2004-02-25 | Boehringer Ingelheim International GmbH | Compositions et méthodes pour le traitement du cancer en utilisant un conjugué d'un anticorps contre le CD44 avec un maytansinoide et des agents chimiothérapeutiques |
US20040062682A1 (en) | 2002-09-30 | 2004-04-01 | Rakow Neal Anthony | Colorimetric sensor |
KR20090088973A (ko) | 2002-10-17 | 2009-08-20 | 젠맵 에이/에스 | Cd20에 대한 인간 모노클로날 항체 |
JP4995423B2 (ja) | 2002-12-03 | 2012-08-08 | ブランシェット・ロックフェラー・ニューロサイエンスィズ・インスティテュート | 物質を血液−脳関門を渡って輸送するための人工低密度リポタンパク質キャリア |
RU2326127C2 (ru) | 2002-12-16 | 2008-06-10 | Джинентех, Инк. | Варианты иммуноглобулинов и их применение |
ES2897506T3 (es) | 2003-01-09 | 2022-03-01 | Macrogenics Inc | Identificación y modificación de anticuerpos con regiones Fc variantes y métodos de utilización de los mismos |
US8367374B2 (en) * | 2003-01-22 | 2013-02-05 | Roche Glycart Ag | Fusion constructs and use of same to produce antibodies with increased Fc receptor binding affinity and effector function |
US8088387B2 (en) | 2003-10-10 | 2012-01-03 | Immunogen Inc. | Method of targeting specific cell populations using cell-binding agent maytansinoid conjugates linked via a non-cleavable linker, said conjugates, and methods of making said conjugates |
AR044388A1 (es) | 2003-05-20 | 2005-09-07 | Applied Molecular Evolution | Moleculas de union a cd20 |
US20040259142A1 (en) | 2003-06-04 | 2004-12-23 | Imperial College Innovations Limited | Products and methods |
EP1639090A4 (fr) | 2003-06-09 | 2008-04-16 | Univ Michigan | Compositions et methodes de traitement et de diagnostic du cancer |
JP4148844B2 (ja) | 2003-06-11 | 2008-09-10 | ソニー・エリクソン・モバイルコミュニケーションズ株式会社 | 情報端末装置及び音声付画像ファイルの出力方法 |
HUE033129T2 (en) * | 2003-07-24 | 2017-11-28 | Innate Pharma Sa | Methods and compositions for increasing the efficacy of therapeutic antibodies using compounds that potentiate NK cells |
WO2005014035A2 (fr) * | 2003-08-08 | 2005-02-17 | Novo Nordisk Health Care Ag | Utilisation de galactose oxydase pour la conjugaison chimique selective de molecules d'extraction a des proteines d'interet therapeutique |
US20050089473A1 (en) | 2003-09-10 | 2005-04-28 | Cedars-Sinai Medical Center | Potassium channel mediated delivery of agents through the blood-brain barrier |
DE602004030810D1 (de) | 2003-09-15 | 2011-02-10 | Smart Tech Lp | Implantate mit befestigten silylierten therapeutischen mitteln |
EP1689439A2 (fr) | 2003-09-22 | 2006-08-16 | Acidophil LLC | Compositions a petites molecules et procedes destines a augmenter l'efficacite d'un medicament au moyen de ces compositions |
US7019288B2 (en) | 2003-09-30 | 2006-03-28 | Sequenom, Inc. | Methods of making substrates for mass spectrometry analysis and related devices |
US20050221337A1 (en) | 2003-10-02 | 2005-10-06 | Massachusetts Institute Of Technology | Microarrays and microspheres comprising oligosaccharides, complex carbohydrates or glycoproteins |
BR122020013239B1 (pt) | 2003-11-05 | 2022-05-10 | Roche Glycart Ag | Anticorpo anti-cd20 humano tipo ii humanizado, seus usos, bem como composição farmacêutica |
KR101520209B1 (ko) | 2003-11-06 | 2015-05-13 | 시애틀 지네틱스, 인크. | 리간드에 접합될 수 있는 모노메틸발린 화합물 |
US20050255491A1 (en) | 2003-11-13 | 2005-11-17 | Lee Frank D | Small molecule and peptide arrays and uses thereof |
JP2007527539A (ja) | 2004-03-05 | 2007-09-27 | ザ スクリプス リサーチ インスティテュート | ハイスループットグリカンマイクロアレイ |
US20050221397A1 (en) | 2004-03-30 | 2005-10-06 | Northern Advancement Center For Science & Technology | RM2 antigen (beta1,4-GalNAc-disialyl-Lc4) as prostate cancer-associated antigen |
EP1740946B1 (fr) | 2004-04-20 | 2013-11-06 | Genmab A/S | Anticorps monoclonaux humains diriges contre cd20 |
ITMI20040928A1 (it) | 2004-05-07 | 2004-08-07 | Uni Di Bologna Dipartiment O D | Procedura per la preparazione di coniugati della doxorubicina con l'albumina umana lattosaminata |
AU2005258281A1 (en) | 2004-06-24 | 2006-01-05 | The Scripps Research Institute | Arrays with cleavable linkers |
KR20190126461A (ko) | 2004-07-22 | 2019-11-11 | 제넨테크, 인크. | Her2 항체 조성물 |
US8022043B2 (en) | 2004-08-27 | 2011-09-20 | Albert Einstein College Of Medicine Of Yeshiva University | Ceramide derivatives as modulators of immunity and autoimmunity |
WO2006060171A2 (fr) | 2004-11-16 | 2006-06-08 | Board Of Regents, The University Of Texas System | Procedes et compositions associes a des ensembles phage-nanoparticule |
WO2006055925A2 (fr) | 2004-11-19 | 2006-05-26 | Swiss Federal Institute Of Technology | Jeux ordonnes de microechantillons pour la detection d'analytes |
WO2006064983A1 (fr) | 2004-12-14 | 2006-06-22 | Korea Research Institute Of Bioscience And Biotechnology | Anticorps monoclonal specifique aux cellules souches embryonnaires humaines |
EP1833489A4 (fr) | 2004-12-28 | 2011-08-03 | Univ Rockefeller | Glycolipides et analogues associes utilises en tant qu'antigenes des lymphocytes nkt |
US7923013B2 (en) | 2004-12-28 | 2011-04-12 | The Rockefeller University | Glycolipids and analogues thereof as antigens for NKT cells |
WO2006072624A2 (fr) | 2005-01-06 | 2006-07-13 | Novo Nordisk A/S | Compositions et procedes de traitement d'infections virales |
US7837990B2 (en) | 2005-03-28 | 2010-11-23 | The Rockefeller University | In vivo expanded NKT cells and methods of use thereof |
CA2603414C (fr) | 2005-03-31 | 2012-09-18 | Biomedics Inc. | Anticorps monoclonal anti-cd-20 |
BRPI0610203A2 (pt) | 2005-05-24 | 2010-06-01 | Avestha Gengraine Tech Pvt Ltd | processo de preparação in vivo de anti-corpo monoclonal anti-cd 20 biologicamente ativo e composição farmacêutica |
US20110129412A1 (en) | 2005-06-02 | 2011-06-02 | Astrazeneca Ab | Antibodies Directed to CD20 and Uses Thereof |
PT1896071E (pt) * | 2005-06-30 | 2015-07-09 | Janssen Biotech Inc | Métodos e composições com melhorias na atividade terapêutica |
JP2007036104A (ja) | 2005-07-29 | 2007-02-08 | Nec Electronics Corp | 半導体装置およびその製造方法 |
JP2009508476A (ja) * | 2005-08-31 | 2009-03-05 | セントカー・インコーポレーテツド | 高められたエフェクター機能をもつ抗体定常領域の製造用の宿主細胞株 |
CA2628255C (fr) | 2005-10-31 | 2016-04-19 | The Regents Of The University Of Michigan | Compositions et methodes pour traiter et diagnostiquer un cancer |
MY149159A (en) | 2005-11-15 | 2013-07-31 | Hoffmann La Roche | Method for treating joint damage |
US7781203B2 (en) | 2005-12-29 | 2010-08-24 | Corning Incorporated | Supports for assaying analytes and methods of making and using thereof |
US20090060921A1 (en) * | 2006-01-17 | 2009-03-05 | Biolex Therapeutics, Inc. | Glycan-optimized anti-cd20 antibodies |
CA2647632C (fr) | 2006-03-27 | 2017-06-27 | University Of Maryland Biotechnology Institute | Synthese de glycoproteines et remodelage par transglycosylation enzymatique |
EA014533B1 (ru) | 2006-05-18 | 2010-12-30 | Ветеринермедицинише Универзитет Вин | Способы обнаружения вирусов гриппа |
EP2035034A4 (fr) | 2006-06-09 | 2009-11-18 | Univ Maryland | Therapie utilisant des anticorps modifies par glycosylation |
JP5215298B2 (ja) | 2006-07-12 | 2013-06-19 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | グリコシル化された基質から切断される末端単糖の固相検出 |
JP2008025989A (ja) | 2006-07-15 | 2008-02-07 | Keio Gijuku | 局在表面プラズモン共鳴法と質量分析法によるリガンドの分析方法及びそのためのセンサー素子 |
CA2660516A1 (fr) | 2006-08-18 | 2008-02-21 | Oncotherapy Science, Inc. | Traitement ou prevention de cancers surexprimant le reg4 ou le kiaa0101 |
AU2007325283B2 (en) | 2006-11-27 | 2012-08-30 | Diadexus, Inc. | Ovr110 antibody compositions and methods of use |
US8765390B2 (en) | 2006-12-08 | 2014-07-01 | The Board Of Trustees Of The Leland Stanford Junior University | Identification and isolation of squamous carcinoma stem cells |
CA2591496C (fr) | 2006-12-18 | 2014-09-02 | Japan Science And Technology Agency | Methode de mesure de l'interaction entre un biomateriau et une chaine glucidique, methode d'evaluation de biomateriau dans la selectivite de la chaine glucidique, methode de tri de biomateriau, methode de prise pour modele de biomateriaux, et trousses de mise en oeuvre |
US20100068806A1 (en) | 2007-01-18 | 2010-03-18 | Suomen Punainen Risti, Veripalvelu | Novel methods and reagents directed to production of cells |
AU2008206887B9 (en) | 2007-01-18 | 2011-07-07 | Glykos Finland Oy | Novel specific cell binders |
CA2675521C (fr) | 2007-01-22 | 2016-04-26 | Raven Biotechnologies | Cellules souches cancereuses humaines |
WO2008103824A1 (fr) | 2007-02-23 | 2008-08-28 | Chinese Academy Of Inspection And Quarantine (Caiq) | Immunoessai à l'or lié à un anticorps par point amélioré en sensibilité pour la détection de virus |
EP2123271B1 (fr) | 2007-03-07 | 2011-10-05 | Daiichi Sankyo Company, Limited | Medicament destine au traitement de la grippe |
US20080220988A1 (en) | 2007-03-07 | 2008-09-11 | Ada Technologies, Inc. | Preparing carbohydrate microarrays and conjugated nanoparticles |
US7960139B2 (en) | 2007-03-23 | 2011-06-14 | Academia Sinica | Alkynyl sugar analogs for the labeling and visualization of glycoconjugates in cells |
EP2125024B1 (fr) | 2007-03-23 | 2013-02-13 | TO-BBB Holding B.V. | Administration intracellulaire ciblée d'agents antiviraux |
US7943330B2 (en) | 2007-03-23 | 2011-05-17 | Academia Sinica | Tailored glycoproteomic methods for the sequencing, mapping and identification of cellular glycoproteins |
US20080260774A1 (en) | 2007-04-13 | 2008-10-23 | Chi-Huey Wong | Alpha-galactosyl ceramide analogs and their use as immunotherapies |
MX2009011500A (es) | 2007-04-23 | 2010-01-29 | Schering Corp | Anticuerpos anti-mdl-1. |
US8082480B2 (en) | 2007-06-27 | 2011-12-20 | Presagis | Distributed checksum computation |
CN101883850B (zh) | 2007-07-12 | 2014-11-12 | 桑格摩生物科学股份有限公司 | 用于失活α-1,6岩藻糖基转移酶(FUT8)基因表达的方法和组合物 |
EP2022848A1 (fr) | 2007-08-10 | 2009-02-11 | Hubrecht Institut | Procédé d'identification, d'expansion, et de suppression de cellules souches adultes et cellules souches de cancer |
CN101828114B (zh) | 2007-08-24 | 2015-03-11 | Lsip基金运营联合公司 | 妇科癌症的检出方法 |
AU2008292859C1 (en) | 2007-08-31 | 2014-03-06 | Academia Sinica | Synthesis of oseltamivir containing phosphonate congeners with anti-influenza activity |
FR2921387B1 (fr) | 2007-09-26 | 2012-04-20 | Sanofi Pasteur | Procede de production du virus de la grippe |
US8647626B2 (en) | 2007-10-02 | 2014-02-11 | Avaxia Biologics, Incorporated | Compositions comprising TNF-specific antibodies for oral delivery |
US20090123439A1 (en) | 2007-11-09 | 2009-05-14 | The Jackson Laboratory | Diagnostic and prognosis methods for cancer stem cells |
WO2009083246A1 (fr) | 2007-12-31 | 2009-07-09 | Bayer Schering Pharma Aktiengesellschaft | Anticorps du tnf alpha |
JP5690713B2 (ja) | 2008-03-21 | 2015-03-25 | ダニスコ・ユーエス・インク | バイオマスの加水分解促進用ヘミセルラーゼ強化組成物 |
EP2272854B1 (fr) | 2008-03-25 | 2015-08-05 | Riken | Nouveau glycolipide et son utilisation |
EP2952897B1 (fr) | 2008-04-09 | 2017-03-22 | Becton, Dickinson and Company | Immunoessais sensibles à l'aide de nanoparticules revêtues |
US8383554B2 (en) | 2008-04-14 | 2013-02-26 | Academia Sinica | Quantitative microarray of intact glycolipid CD1d interaction and correlation with cell-based cytokine production |
US7846744B2 (en) * | 2008-04-22 | 2010-12-07 | Ravetch Jeffrey V | Methods of identifying anti-inflammatory compounds |
US8906832B2 (en) | 2008-04-30 | 2014-12-09 | Academia Sinica | Quantitative analysis of carbohydrate-protein interactions using glycan microarrays: determination of surface and solution dissociation constants |
CN105363034A (zh) | 2008-05-23 | 2016-03-02 | 香港大学 | 治疗流感的联合疗法 |
US20110137570A1 (en) * | 2008-05-30 | 2011-06-09 | Anthony Lapadula | Methods for structural analysis of glycans |
AU2009268937A1 (en) | 2008-06-16 | 2010-01-14 | Aj Park | Compositions for inducing immune responses specific to Globo H and SSEA3 and uses thereof in cancer treatment |
CN102066940B (zh) | 2008-06-16 | 2015-05-13 | 中央研究院 | 根据对抗Globo H及其片段的抗体量的癌症诊断 |
JP2010014691A (ja) | 2008-06-20 | 2010-01-21 | Igaku Seibutsugaku Kenkyusho:Kk | 腹水中のメソテリン及び/又は巨核球増強因子を検出するための方法、キット、試薬及び装置 |
US20100003674A1 (en) | 2008-07-03 | 2010-01-07 | Cope Frederick O | Adult stem cells, molecular signatures, and applications in the evaluation, diagnosis, and therapy of mammalian conditions |
US7928077B2 (en) | 2008-07-11 | 2011-04-19 | Academia Sinica | Alpha-galactosyl ceramide analogs and their use as immunotherapies |
WO2010009271A2 (fr) | 2008-07-15 | 2010-01-21 | Academia Sinica | Matrices de glycane sur des lames de verre revêtues d’aluminium de type ptfe et procédés associés |
US20100022916A1 (en) | 2008-07-24 | 2010-01-28 | Javanbakhsh Esfandiari | Method and Apparatus for Collecting and Preparing Biological Samples for Testing |
GB0816679D0 (en) | 2008-09-11 | 2008-10-22 | Univ Bath | Compounds for treating viral infections |
US8080415B2 (en) | 2008-09-26 | 2011-12-20 | Eureka Therapeutics, Inc. | Modified host cells and uses thereof |
WO2010050190A1 (fr) | 2008-10-27 | 2010-05-06 | 北海道公立大学法人札幌医科大学 | Marqueur moléculaire de cellule souche cancéreuse |
AR074196A1 (es) * | 2008-11-17 | 2010-12-29 | Genentech Inc | Metodo y formulacion para reducir la agregacion de una macromolecula bajo condiciones fisiologicas |
SG173796A1 (en) * | 2009-02-25 | 2011-09-29 | Merck Sharp & Dohme | Metabolic engineering of a galactose assimilation pathway in the glycoengineered yeast pichia pastoris |
ES2555220T3 (es) | 2009-03-27 | 2015-12-29 | Academia Sinica | Donantes de sialil-fosfato selectivos para la preparación de sialósidos y matrices de sialósidos para la detección del virus de la gripe |
EP2427211A4 (fr) * | 2009-05-04 | 2013-05-01 | Abbott Biotech Ltd | Formulations stables à concentration protéique élevée d'anticorps anti-tnf-alpha humain |
WO2011005756A1 (fr) | 2009-07-06 | 2011-01-13 | Puretech Ventures, Llc | Administration d'agents ciblés contre des niches de microbiote |
AU2010273118B2 (en) | 2009-07-15 | 2015-10-29 | The University Of British Columbia | 2,3-fluorinated glycosides as neuraminidase inhibitors and their use as anti-virals |
BR112012001395A2 (pt) | 2009-07-22 | 2019-09-24 | Enzon Pharmaceuticals Inc | metodo para tratar um câncer her2 positivo em um mamifero metodo para aumentar os efetivos de antagonistas do receptor her2 em um mamifero apresentando um cancêr her2 positivo metodo para inibir o crescimento ou proliferação de células her2 positivas em um mamifero |
WO2011031236A1 (fr) | 2009-09-14 | 2011-03-17 | Thailand Excellence Center For Tissue Engineering | Compositions phytochimiques comprenant des xanthones destinées à combattre une tempête de cytokines inflammatoires, et autres utilisations |
US10087236B2 (en) | 2009-12-02 | 2018-10-02 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
WO2011074621A1 (fr) | 2009-12-18 | 2011-06-23 | 株式会社医学生物学研究所 | Anticorps contre la mesotheline (msln), et mise en œuvre de celui-ci |
EP2347769A1 (fr) | 2010-01-20 | 2011-07-27 | Glycotope GmbH | Marqueurs de cellules souches de cancer et utilisations associées |
CA2789623A1 (fr) | 2010-02-11 | 2011-08-18 | Alexion Pharmaceutical, Inc. | Methodes therapeutiques faisant appel aux anticorps anti-cd200 |
CN102858949B (zh) | 2010-02-24 | 2016-07-06 | 默沙东公司 | 用于增加在巴氏毕赤酵母中生产的治疗性糖蛋白上的n-糖基化位点占据的方法 |
AR080513A1 (es) | 2010-03-12 | 2012-04-11 | Inmunogen Inc | Moleculas de union cd37 y sus inmunoconjugados |
WO2011130332A1 (fr) | 2010-04-12 | 2011-10-20 | Academia Sinica | Puces au glycane pour la recherche par criblage haut débit de virus |
EP2558571A4 (fr) | 2010-04-16 | 2014-09-24 | Immune Disease Inst Inc | Expression de polypeptide prolongée à partir d'arn synthétiques modifiés et utilisations de celle-ci |
WO2011143262A2 (fr) | 2010-05-10 | 2011-11-17 | Sinica, Academia | Congénères de phosphonate de zanamivir ayant une activité antigrippale et détermination de la sensibilité à l'oseltamivir d'influenzavirus |
WO2011145957A1 (fr) | 2010-05-20 | 2011-11-24 | Auckland Uniservices Limited | Agents et procédés de détection et/ou d'imagerie d'hypoxie |
BR112012030179A8 (pt) * | 2010-05-27 | 2023-03-14 | Merck Sharp & Dohme | Polipeptídeo contendo fc |
GB201015569D0 (en) | 2010-09-16 | 2010-10-27 | Medical Res Council | Blood assay for prions |
WO2012082635A1 (fr) | 2010-12-13 | 2012-06-21 | Ancora Pharmaceuticals, Inc. | Streptocoque du groupe a à base d'oligosaccharides synthétiques |
BR112013017382B1 (pt) | 2011-01-05 | 2021-03-16 | National Taiwan University | método de preparação de um composto de fórmula (5) |
WO2012116432A1 (fr) | 2011-02-28 | 2012-09-07 | Mcmaster University | Traitement du cancer par des antagonistes des récepteurs dopaminergiques |
US10851174B2 (en) | 2011-03-03 | 2020-12-01 | University Of Maryland, Baltimore | Core fucosylated glycopeptides and glycoproteins: chemoenzymatic synthesis and uses thereof |
WO2012162277A1 (fr) | 2011-05-25 | 2012-11-29 | Merck Sharp & Dohme Corp. | Procédé de préparation de polypeptides contenant fc à propriétés améliorées |
LT3418300T (lt) | 2011-07-18 | 2021-01-11 | Institute For Research In Biomedicine | Neutralizuojantys antikūnai prieš gripo virusą a ir jų panaudojimas |
WO2013012066A1 (fr) | 2011-07-21 | 2013-01-24 | 京セラ株式会社 | Dispositif d'éclairage, tête de capteur d'image et dispositif de lecture le comprenant |
CA2841458C (fr) | 2011-08-12 | 2019-07-16 | Nissan Chemical Industries, Ltd. | Composes heterocycliques tricycliques et inhibiteurs de jak |
CA2853809A1 (fr) * | 2011-10-31 | 2013-05-10 | Merck Sharp & Dohme Corp. | Procede de preparation d'anticorps possedant des proprietes ameliorees |
WO2013074598A1 (fr) | 2011-11-18 | 2013-05-23 | Merck Sharp & Dohme Corp. | Polypeptides contenant fc ayant des propriétés anti-inflammatoires améliorées et une liaison améliorée à fcrn |
EP2604281B1 (fr) | 2011-12-14 | 2014-07-30 | Centre National de la Recherche Scientifique (CNRS) | Analogues conjugués de somatostatine coupés pour des applications biologiques |
WO2013106937A1 (fr) | 2012-01-19 | 2013-07-25 | The University Of British Columbia | Composés inhibiteurs de la neuraminidase substitués par le fluor 3' équatorial, compositions et méthodes |
GB201201314D0 (en) | 2012-01-26 | 2012-03-07 | Isis Innovation | Composition |
CA2862925C (fr) * | 2012-02-10 | 2020-01-21 | University Of Maryland, Baltimore | Glyco-ingenierie chimio-enzymatique d'anticorps et de leurs fragments fc |
US9846160B2 (en) | 2012-02-27 | 2017-12-19 | Board Of Regents, The University Of Texas Systems | Ganglioside GD2 as a marker and target on cancer stem cells |
US20150231219A1 (en) | 2012-04-02 | 2015-08-20 | Merrimack Pharmaceuticals, Inc. | Dosage and administration of monospecific and bispecific anti-igr-1r and anti-erbb3 antibodies |
WO2013151649A1 (fr) | 2012-04-04 | 2013-10-10 | Sialix Inc | Composés d'interaction avec des glycanes |
US10130714B2 (en) | 2012-04-14 | 2018-11-20 | Academia Sinica | Enhanced anti-influenza agents conjugated with anti-inflammatory activity |
EP2855745A4 (fr) | 2012-06-01 | 2016-01-20 | Momenta Pharmaceuticals Inc | Méthodes associées à l'adalimumab |
AU2013306098A1 (en) | 2012-08-18 | 2015-02-12 | Academia Sinica | Cell-permeable probes for identification and imaging of sialidases |
TWI573876B (zh) | 2012-08-20 | 2017-03-11 | 中央研究院 | 寡醣之大規模酵素合成 |
US9547009B2 (en) | 2012-08-21 | 2017-01-17 | Academia Sinica | Benzocyclooctyne compounds and uses thereof |
WO2014070957A1 (fr) | 2012-10-30 | 2014-05-08 | Esperance Pharmaceuticals, Inc. | Conjugués anticorps/médicament et leurs procédés d'utilisation |
JP6506024B2 (ja) * | 2012-11-05 | 2019-04-24 | 全薬工業株式会社 | 抗体又は抗体組成物の製造方法 |
WO2014078373A1 (fr) | 2012-11-13 | 2014-05-22 | Iogenetics, Llc | Compositions antimicrobiennes |
CN103045647A (zh) * | 2012-11-29 | 2013-04-17 | 大连大学 | 核心岩藻糖基转移酶基因沉默细胞模型的建立及鉴定方法 |
GB201305986D0 (en) | 2013-04-03 | 2013-05-15 | Asociaci N Ct De Investigaci N Cooperativa En Biomateriales | Synthesis and use of isotopically-labelled glycans |
EP2983720B1 (fr) | 2013-04-13 | 2018-08-01 | Universidade de Coimbra | Plateforme pour l'administration ciblée à des cellules tumorales et son utilisation |
CN104225616A (zh) | 2013-06-08 | 2014-12-24 | 中南大学 | 一种靶向卵巢癌干细胞的抗肿瘤生物制剂 |
EP3013365B1 (fr) | 2013-06-26 | 2019-06-05 | Academia Sinica | Antigènes rm2 et leur utilisation |
WO2014210564A1 (fr) | 2013-06-27 | 2014-12-31 | Academia Sinica | Conjugués de glycane et leur utilisation |
TWI599370B (zh) * | 2013-07-26 | 2017-09-21 | 中央研究院 | 靈芝多醣誘發之抗體介導抗腫瘤活性 |
AU2014317092B2 (en) | 2013-09-05 | 2018-02-08 | Universiteit Gent | Cells producing Fc containing molecules having altered glycosylation patterns and methods and use thereof |
CA2923579C (fr) | 2013-09-06 | 2023-09-05 | Academia Sinica | Activation des cellules humaines inkt a l'aide de glycolipides ayant des groupes glycolsyles modifies |
JP2016530892A (ja) | 2013-09-12 | 2016-10-06 | テバ ファーマシューティカル インダストリーズ リミティド | ラキニモド応答性を有する遺伝子発現バイオマーカー |
CN103436627B (zh) | 2013-09-13 | 2016-02-03 | 四川大学华西医院 | 一种恶性乳腺癌干细胞的筛查试剂盒 |
WO2015054039A1 (fr) * | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Polypeptides contenant fc présentant une liaison accrue à fcgammariib |
US9982041B2 (en) * | 2014-01-16 | 2018-05-29 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US10150818B2 (en) | 2014-01-16 | 2018-12-11 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
TWI682033B (zh) * | 2014-03-17 | 2020-01-11 | 泉盛生物科技股份有限公司 | 製造具有經修飾的糖苷化作用之重組糖蛋白之方法 |
EP3129767B1 (fr) | 2014-03-27 | 2021-09-01 | Academia Sinica | Composés de marquage réactifs et leurs utilisations |
US10118969B2 (en) | 2014-05-27 | 2018-11-06 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
AU2015267047A1 (en) | 2014-05-27 | 2017-01-05 | Academia Sinica | Anti-CD20 glycoantibodies and uses thereof |
AU2015267052A1 (en) | 2014-05-27 | 2016-12-15 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
JP7062361B2 (ja) | 2014-05-27 | 2022-05-06 | アカデミア シニカ | 抗her2糖操作抗体群およびその使用 |
JP7063538B2 (ja) * | 2014-05-28 | 2022-05-09 | アカデミア シニカ | 抗TNFα糖操作抗体群およびその使用 |
JP6588084B2 (ja) | 2014-08-19 | 2019-10-09 | ミルテニイ バイオテック ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ssea4抗原に特異的なキメラ抗原受容体 |
TWI587871B (zh) | 2014-08-22 | 2017-06-21 | 中央研究院 | 新穎之聚醣共軛物及其用途 |
WO2016040369A2 (fr) | 2014-09-08 | 2016-03-17 | Academia Sinica | Activation des cellules inkt humaines par des glycolipides |
CA2960282A1 (fr) | 2014-09-12 | 2016-03-17 | The Regents Of The University Of California | Anticorps anti-cd46 humains formant des macropinosomes et agents therapeutiques anti-cancereux cibles |
US10495645B2 (en) | 2015-01-16 | 2019-12-03 | Academia Sinica | Cancer markers and methods of use thereof |
US9975965B2 (en) | 2015-01-16 | 2018-05-22 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
WO2016118090A1 (fr) | 2015-01-23 | 2016-07-28 | Agency For Science, Technology And Research | Protéines de liaison à l'antigène spécifiques du cancer |
CA2972072A1 (fr) | 2015-01-24 | 2016-07-28 | Academia Sinica | Nouveaux composes conjugues de glycane et leurs methodes d'utilisation |
EP3250590B1 (fr) * | 2015-01-30 | 2021-09-15 | Academia Sinica | Compositions et procédés concernant des glycoformes universelles pour une efficacité d'anticorps anti-ssea4 améliorée |
US20170283878A1 (en) | 2015-12-11 | 2017-10-05 | Academia Sinica | Modulation of globoseries glycosphingolipid synthesis and cancer biomarkers |
TW201808978A (zh) | 2016-03-08 | 2018-03-16 | 中央研究院 | N-聚醣及其陣列之模組化合成方法 |
KR20180121786A (ko) | 2016-03-29 | 2018-11-08 | 오비아이 파머 인코퍼레이티드 | 항체, 제약 조성물 및 방법 |
AU2017316663B2 (en) | 2016-08-22 | 2024-02-22 | CHO Pharma Inc. | Antibodies, binding fragments, and methods of use |
CN110234341A (zh) | 2016-08-24 | 2019-09-13 | 醣基生医股份有限公司 | 利用糖苷内切酶突变体重塑糖蛋白及其使用方法 |
EP3541414B1 (fr) | 2016-11-21 | 2024-08-28 | OBI Pharma, Inc. | Molécules biologiques conjuguées, compositions pharmaceutiques et procédés |
WO2020006176A1 (fr) | 2018-06-27 | 2020-01-02 | Obi Pharma, Inc. | Variants de glycosynthases pour génie des glycoprotéines et leurs procédés d'utilisation |
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US11377485B2 (en) * | 2009-12-02 | 2022-07-05 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
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